Congenital stationary night blindness, type 1B Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/257270
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Genes

1 genes associated with the Congenital stationary night blindness, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
GRM6 glutamate receptor, metabotropic 6